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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739437Generated: November 1, 2026

Acetic Anhydride → 4-(3,4-diethoxybenzylidene)-2-methyloxazol-5(4H)-one

https://huagongshe.com/reaction/1739437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantAcetylglycineHCID 10972—
Reactant3,4-DiethoxybenzaldehydeHCID 74847—
ReactantSodium AcetateHCID 517045—
SolventWaterHCID 962—
Product4-(3,4-diethoxybenzylidene)-2-methyloxazol-5(4H)-oneHCID 5443353545%

Reaction Steps

To acetic anhydride (193 ml) are added 3,4-diethoxybenzaldehyde (234.4 g), N-acetylglycine (95.4 g) and sodium acetate (49.5 g), and the mixture is heated under reflux for one hour, and the reaction mixture is allowed to stand for cooling. The reaction mixture is further allowed to stand in a refrigerator overnight, and then thereto is added water. The mixture is extracted with chloroform, and the extract is washed, dried and concentrated. The residue is crystallized from ethanol to give 4-(3,4-diethoxybenzylidene)-2-methyloxazol-5(4H)-one (100.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965730
Source datasetuspto-grants-1999_10
ORD IDord-9f5164a76cf441b7a949db897de885d5
Source noteuspto-grants-1999_10